JSON

autosomal recessive congenital cerebellar ataxia

Go to external page http://purl.obolibrary.org/obo/MONDO_0020043

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C5681519 (MONDO:equivalentTo)
  • MEDGEN:1843070 (MONDO:equivalentTo)
  • Orphanet:98095 (MONDO:equivalentTo)
  • GARD:19412 (MONDO:GARD)
Subsets

matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, otar, disease_grouping, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, mondo_top_grouping_member, mondo_top_grouping_hereditary_disease, nord_rare, matrix_included, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_hereditary_disease, ordo_group_of_disorders, harrisons_view_nervous_system_disorder

exactMatch

http://www.orpha.net/ORDO/Orphanet_98095

http://linkedlifedata.com/resource/umls/id/C5681519

http://identifiers.org/medgen/1843070

id

MONDO:0020043

Term relations